regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3270): Show |
intron_variant | MODIFIER | NA18953.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0015 | 1 | 290 | 0.0035 | 3277 | c.162 others(3296): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3270): Show |
intron_variant | MODIFIER | NA18961.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0058 | 1 | 290 | 0.0035 | 3277 | c.162 others(3296): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3270): Show |
intron_variant | MODIFIER | NA18948.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0044 | 1 | 290 | 0.0035 | 3277 | c.162 others(3296): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
EHMT1_chr9_137614005_137841127 | 137716335 | G | GTGGTGTC others(3270): Show |
intron_variant | MODIFIER | NA18979.hp2 | a0001 | a0001c0011 | a0001c0011t0001 | a0001c0011t0001g0034 | 1 | 170 | 0.0059 | 3277 | c.86- others(3290): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
MEGF6_chr1_3482951_3616508 | 3502017 | G | GCCTCACA others(3270): Show |
intron_variant | MODIFIER | HG02165.hp2 | a0007 | a0007c0008 | a0007c0008t0001 | a0007c0008t0001g0133 | 1 | 292 | 0.0034 | 3277 | c.218 others(3292): Show |
MEGF6 | ENSG00000162591.17 | transcript | ENST00000356575.9 | protein_coding | 17/36 | chr1 | TogoVar | ||||||
MYO3B_chr2_170173147_170660167 | 170511323 | C | CCCAAAGT others(3270): Show |
intron_variant | MODIFIER | HG00733.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0153 | 1 | 174 | 0.0058 | 3277 | c.337 others(3296): Show |
MYO3B | ENSG00000071909.19 | transcript | ENST00000408978.9 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
SPECC1_chr17_20004359_20324026 | 20092293 | G | GGAAATCA others(3270): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0003 | a0001c0003t0062 | a0001c0003t0062g0242 | 1 | 250 | 0.0040 | 3277 | c.-21 others(3294): Show |
SPECC1 | ENSG00000128487.19 | transcript | ENST00000395527.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
SPECC1_chr17_20004359_20324026 | 20092293 | G | GGAAATCA others(3270): Show |
intron_variant | MODIFIER | HG02559.hp2 | a0001 | a0001c0003 | a0001c0003t0021 | a0001c0003t0021g0198 | 1 | 250 | 0.0040 | 3277 | c.-21 others(3294): Show |
SPECC1 | ENSG00000128487.19 | transcript | ENST00000395527.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ALDH16A1_chr19_49448225_49476050 | 49461541 | G | GAGTCTGG others(3271): Show |
intron_variant | MODIFIER | HG02132.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0177 | 1 | 342 | 0.0029 | 3278 | c.578 others(3291): Show |
ALDH16A1 | ENSG00000161618.10 | transcript | ENST00000293350.9 | protein_coding | 5/16 | chr19 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3271): Show |
intron_variant | MODIFIER | NA18971.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0050 | 1 | 290 | 0.0035 | 3278 | c.162 others(3297): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3271): Show |
intron_variant | MODIFIER | NA19012.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0032 | 1 | 290 | 0.0035 | 3278 | c.162 others(3297): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3271): Show |
intron_variant | MODIFIER | HG03710.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0049 | 1 | 290 | 0.0035 | 3278 | c.162 others(3297): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3271): Show |
intron_variant | MODIFIER | HG00323.hp1 NA20300.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0047a0001c0001t0003g0026 | 2 | 290 | 0.0069 | 3278 | c.162 others(3297): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3271): Show |
intron_variant | MODIFIER | HG01952.hp2 HG02083.hp1 NA18951.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0029others(5): Show | 8 | 290 | 0.0276 | 3278 | c.162 others(3297): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3271): Show |
intron_variant | MODIFIER | NA18943.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0022 | 1 | 290 | 0.0035 | 3278 | c.162 others(3297): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
IFNAR1_chr21_33319970_33364864 | 33322690 | C | CGGAATGT others(3271): Show |
upstream_gene_variant | MODIFIER | HG02698.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0175 | 1 | 323 | 0.0031 | 3278 | c.-23 others(3289): Show |
IFNAR1 | ENSG00000142166.15 | transcript | ENST00000270139.8 | protein_coding | 2279 | chr21 | TogoVar | ||||||
IFNAR1_chr21_33319970_33364864 | 33322912 | T | TATATATA others(3271): Show |
upstream_gene_variant | MODIFIER | HG03834.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | 1 | 323 | 0.0031 | 3278 | c.-21 others(3289): Show |
IFNAR1 | ENSG00000142166.15 | transcript | ENST00000270139.8 | protein_coding | 2057 | chr21 | TogoVar | ||||||
SHC2_chr19_411589_466033 | 433448 | G | GATAGATG others(3271): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0046 | 1 | 212 | 0.0047 | 3278 | c.111 others(3297): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | TogoVar | ||||||
ABR_chr17_998519_1184981 | 1065141 | C | CTGTTACG others(3272): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0001 | a0001c0001 | a0001c0001t0045 | a0001c0001t0045g0247 | 1 | 337 | 0.0030 | 3279 | c.118 others(3298): Show |
ABR | ENSG00000159842.16 | transcript | ENST00000302538.10 | protein_coding | 10/22 | chr17 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3477303 | G | GTCACCCC others(3272): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0002 | a0002c0012 | a0002c0012t0010 | a0002c0012t0010g0277 | 1 | 334 | 0.0030 | 3279 | c.147 others(3296): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3272): Show |
intron_variant | MODIFIER | HG01169.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0037 | 1 | 290 | 0.0035 | 3279 | c.162 others(3298): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3272): Show |
intron_variant | MODIFIER | NA18994.hp1 NA18995.hp1 NA19004.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0001g0068 | 3 | 290 | 0.0103 | 3279 | c.162 others(3298): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3272): Show |
intron_variant | MODIFIER | NA18947.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0043 | 1 | 290 | 0.0035 | 3279 | c.162 others(3298): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3272): Show |
intron_variant | MODIFIER | NA18747.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0060 | 1 | 290 | 0.0035 | 3279 | c.162 others(3298): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3272): Show |
intron_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0063 | 1 | 290 | 0.0035 | 3279 | c.162 others(3298): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
EHMT1_chr9_137614005_137841127 | 137721342 | A | ACTCGCCC others(3272): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0066 | 1 | 170 | 0.0059 | 3279 | c.642 others(3296): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
IQSEC3_chr12_61767_183455 | 163273 | C | CCCTCCAC others(3272): Show |
intron_variant | MODIFIER | HG02698.hp2 HG03688.hp1 NA20905.hp2 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0133a0001c0002t0002g0137a0001c0002t0002g0167 | 3 | 282 | 0.0106 | 3279 | c.258 others(3296): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM242_chr6_157284025_157328519 | 157311511 | C | CCCCATTG others(3272): Show |
intron_variant | MODIFIER | HG00099.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0045 | 1 | 344 | 0.0029 | 3279 | c.327 others(3296): Show |
TMEM242 | ENSG00000215712.11 | transcript | ENST00000400788.9 | protein_coding | 3/3 | chr6 | TogoVar | ||||||
ZBTB42_chr14_104796101_104809712 | 104806614 | A | ACCACCAT others(3272): Show |
downstream_gene_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0000 | 1 | 99 | 0.0101 | 3279 | c.*41 others(3290): Show |
ZBTB42 | ENSG00000179627.10 | transcript | ENST00000342537.8 | protein_coding | 1903 | chr14 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCACCG others(3273): Show |
intron_variant | MODIFIER | HG02129.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0028 | 1 | 290 | 0.0035 | 3280 | c.162 others(3299): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3273): Show |
intron_variant | MODIFIER | NA19063.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 | 1 | 290 | 0.0035 | 3280 | c.162 others(3299): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3273): Show |
intron_variant | MODIFIER | NA18991.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0018 | 1 | 290 | 0.0035 | 3280 | c.162 others(3299): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3273): Show |
intron_variant | MODIFIER | HG02155.hp1 | a0001 | a0001c0001 | a0001c0001t0032 | a0001c0001t0032g0013 | 1 | 290 | 0.0035 | 3280 | c.162 others(3299): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3273): Show |
intron_variant | MODIFIER | NA19003.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0064 | 1 | 290 | 0.0035 | 3280 | c.162 others(3299): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3273): Show |
intron_variant | MODIFIER | NA18950.hp1 | a0001 | a0001c0001 | a0001c0001t0034 | a0001c0001t0034g0055 | 1 | 290 | 0.0035 | 3280 | c.162 others(3299): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3273): Show |
intron_variant | MODIFIER | HG01168.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 290 | 0.0035 | 3280 | c.162 others(3299): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3273): Show |
intron_variant | MODIFIER | NA19057.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0048 | 1 | 290 | 0.0035 | 3280 | c.162 others(3299): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3273): Show |
intron_variant | MODIFIER | NA19065.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0040 | 1 | 290 | 0.0035 | 3280 | c.162 others(3299): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3273): Show |
intron_variant | MODIFIER | HG01943.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0042 | 1 | 290 | 0.0035 | 3280 | c.162 others(3299): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
IQSEC3_chr12_61767_183455 | 163272 | C | CCCCTCCA others(3273): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0001 | a0001c0002 | a0001c0002t0047 | a0001c0002t0047g0201 | 1 | 282 | 0.0036 | 3280 | c.258 others(3297): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
MEGF6_chr1_3482951_3616508 | 3502017 | G | GCCTCACA others(3273): Show |
intron_variant | MODIFIER | HG02109.hp2 | a0037 | a0037c0027 | a0037c0027t0034 | a0037c0027t0034g0271 | 1 | 292 | 0.0034 | 3280 | c.218 others(3295): Show |
MEGF6 | ENSG00000162591.17 | transcript | ENST00000356575.9 | protein_coding | 17/36 | chr1 | TogoVar | ||||||
SLC38A10_chr17_81239811_81300307 | 81249456 | G | GAGGAGGG others(3273): Show |
intron_variant | MODIFIER | NA19077.hp2 | a0002 | a0002c0001 | a0002c0001t0002 | a0002c0001t0002g0100 | 1 | 214 | 0.0047 | 3280 | c.206 others(3299): Show |
SLC38A10 | ENSG00000157637.13 | transcript | ENST00000374759.8 | protein_coding | 14/15 | chr17 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045866 | T | TTCCTCCA others(3274): Show |
intron_variant | MODIFIER | HG02723.hp1 HG02809.hp2 |
a0003 | a0003c0011 | a0003c0011t0006 | a0003c0011t0006g0030 | 2 | 390 | 0.0051 | 3281 | c.109 others(3296): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3274): Show |
intron_variant | MODIFIER | NA19074.hp2 | a0003 | a0003c0009 | a0003c0009t0002 | a0003c0009t0002g0054 | 1 | 290 | 0.0035 | 3281 | c.162 others(3300): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
DYM_chr18_49031387_49465645 | 49203061 | G | GCCCCCCG others(3274): Show |
intron_variant | MODIFIER | HG02523.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023 | 1 | 290 | 0.0035 | 3281 | c.162 others(3300): Show |
DYM | ENSG00000141627.14 | transcript | ENST00000675505.1 | protein_coding | 14/17 | chr18 | TogoVar | ||||||
MSH3_chr5_80649652_80881815 | 80803524 | T | TCTCTTCA others(3274): Show |
intron_variant | MODIFIER | NA18978.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0039 | 1 | 362 | 0.0028 | 3281 | c.265 others(3302): Show |
MSH3 | ENSG00000113318.11 | transcript | ENST00000265081.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
SERPINF2_chr17_1737871_1760265 | 1740324 | A | AGCCGGAC others(3274): Show |
upstream_gene_variant | MODIFIER | HG03041.hp2 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0042a0001c0001t0004g0042 | 2 | 445 | 0.0045 | 3281 | c.-25 others(3292): Show |
SERPINF2 | ENSG00000167711.14 | transcript | ENST00000453066.6 | protein_coding | 2546 | chr17 | TogoVar | ||||||
SERPINF2_chr17_1737871_1760265 | 1740324 | A | AGCCGGAC others(3274): Show |
upstream_gene_variant | MODIFIER | HG04199.hp1 | a0002 | a0002c0002 | a0002c0002t0004 | a0002c0002t0004g0085 | 1 | 445 | 0.0023 | 3281 | c.-25 others(3292): Show |
SERPINF2 | ENSG00000167711.14 | transcript | ENST00000453066.6 | protein_coding | 2546 | chr17 | TogoVar | ||||||
WDR81_chr17_1719704_1743585 | 1740324 | A | AGCCGGAC others(3274): Show |
downstream_gene_variant | MODIFIER | HG03041.hp1 NA18522.hp1 |
a0001a0025 | a0001c0037a0025c0067 | a0001c0037t0003a0025c0067t0003 | a0001c0037t0003g0058a0025c0067t0003g0002 | 2 | 431 | 0.0046 | 3281 | c.*26 others(3292): Show |
WDR81 | ENSG00000167716.19 | transcript | ENST00000409644.6 | protein_coding | 1740 | chr17 | TogoVar | ||||||
WDR81_chr17_1719704_1743585 | 1740324 | A | AGCCGGAC others(3274): Show |
downstream_gene_variant | MODIFIER | HG04199.hp1 | a0003 | a0003c0004 | a0003c0004t0003 | a0003c0004t0003g0016 | 1 | 431 | 0.0023 | 3281 | c.*26 others(3292): Show |
WDR81 | ENSG00000167716.19 | transcript | ENST00000409644.6 | protein_coding | 1740 | chr17 | TogoVar |